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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112767copy number variation1nstd102humanPathogenic GRCh37 chr8: 143,958,418-143,996,344 , GRCh38.p12 chr8: 142,877,002-142,914,928 CYP11B1, CYP11B2
    nsv5372176translocation1nstd200human GRCh38 chr8: 142,915,434-142,915,434 , GRCh38 chr8: 142,877,832-142,877,832 , GRCh37.p13 chr8: 143,959,248-143,959,248 , GRCh37.p13 chr8: 143,996,850-143,996,850 CYP11B1, CYP11B2
    nsv4969152copy number variation1nstd200human GRCh38 chr8: 142,873,360-142,911,106 , GRCh37.p13 chr8: 143,954,776-143,992,522 CYP11B1, CYP11B2
    nsv4889324inversion1nstd200human GRCh37 chr8: 143,957,119-143,957,719 , GRCh38.p12 chr8: 142,875,703-142,876,303 CYP11B1
    nsv4681791copy number variation1nstd102humanPathogenic GRCh37 chr8: 143,955,779-143,999,600 , GRCh38.p12 chr8: 142,874,363-142,918,184 CYP11B1, CYP11B2
    nsv4676049copy number variation1nstd102humanPathogenic GRCh37 chr8: 143,616,831-144,930,611 , GRCh38.p12 chr8: 142,535,470-143,848,439 PYCR3, MROH4P, 69 more genes
    nsv4675692copy number variation1nstd102humanUncertain significance GRCh37 chr8: 143,570,920-144,459,613 , GRCh38.p12 chr8: 142,489,559-143,377,443 SLURP2, THEM6, 37 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4675029copy number variation1nstd102humanPathogenic GRCh37 chr8: 142,132,678-145,569,441 , GRCh38.p12 chr8: 141,122,579-144,345,779 RHPN1-AS1, MIR6847, 117 more genes
    nsv4674889copy number variation1nstd102humanUncertain significance GRCh37 chr8: 143,728,492-144,093,928 , GRCh38.p12 chr8: 142,647,108-143,012,511 THEM6, LNCOC1, 16 more genes
    nsv4614227copy number variation1nstd183human GRCh37 chr8: 143,958,395-143,958,451 , GRCh38.p12 chr8: 142,876,979-142,877,035 CYP11B1
    nsv4608284copy number variation1nstd183human GRCh37 chr8: 143,956,514-143,956,576 , GRCh38.p12 chr8: 142,875,098-142,875,160 CYP11B1
    nsv4607223copy number variation1nstd183human GRCh37 chr8: 143,958,395-143,958,604 , GRCh38.p12 chr8: 142,876,979-142,877,188 CYP11B1
    nsv4457078copy number variation1nstd102humanPathogenic GRCh37 chr8: 139,188,797-146,295,771 , GRCh38.p12 chr8: 138,176,554-145,070,385 GSDMD, MROH1, 181 more genes
    nsv4456997copy number variation1nstd102humanPathogenic GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385 LOC107986906, GPIHBP1, 317 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456783copy number variation1nstd102humanPathogenic GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385 HAS2, ZNF696, 369 more genes
    nsv4456284copy number variation1nstd102humanUncertain significance GRCh37 chr8: 143,786,100-143,964,656 , GRCh38.p12 chr8: 142,704,682-142,883,240 CYP11B1, LY6D, 10 more genes
    nsv4456083copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,988,974-144,218,537 , GRCh38.p12 chr8: 141,907,613-143,137,120 LY6E, CYP11B2, 32 more genes
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